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{"sheet":"Лист1","index":0,"n_rows":31,"n_cols":9,"rows_kept":31,"cut":false,"hidden":false,"merged":[]}
["Damaging mutations"]
["Protein","Position","AA1","AA2","Protein_uniprot","gene_name","Nucleotides","link to OMIA entry","Disease"]
["F6R4K5",210,"H","R","F6R4K5_BOVIN","TUBD1","rs383232842[T>C]","http://omia.angis.org.au/OMIA001939/9913/","Abortion due to haplotype BH2"]
["Q2KIK0",317,"W","R","SGT1_BOVIN","SUGT1","949T>C","http://omia.angis.org.au/OMIA001960/9913/","Abortion due to haplotype FH4"]
["Q59A32",290,"N","T","PUR2_BOVIN","GART","g.1277227A.C","http://omia.angis.org.au/OMIA001826/9913/","Abortion due to haplotype HH4"]
["Q5E9B3",195,"Y","C","PGTB2_BOVIN","RABGGTB","na","http://omia.angis.org.au/OMIA002037/9913/","Abortion (embryonic lethality), RABGGTB-related"]
["P02666",82,"P","H","CASB_BOVIN","CSN2","c.245A>C","http://omia.angis.org.au/OMIA002033/9913/","A2 milk"]
["A6QP89",295,"L","R","A6QP89_BOVIN","MYBPC1","c.885T>G","http://omia.angis.org.au/OMIA001978/9913/","Arthrogryposis, distal, type 1B"]
["Q9TTK4",2015,"H","R","LYST_BOVIN","LYST","A_to_G","http://omia.angis.org.au/OMIA000185/9913/","Chediak-Higashi syndrome"]
["Q6YC49",180,"V","F","S35A3_BOVIN","SLC35A3","c.559G>T","http://omia.angis.org.au/OMIA001340/9913/","Complex vertebral malformation"]
["Q0VCY0",559,"R","C","AT2A1_BOVIN","ATP2A1","C1676T","http://omia.angis.org.au/OMIA001450/9913/","Congenital muscular dystonia 1"]
["F1N5R0",270,"L","P","F1N5R0_BOVIN","LOC528050","T809C","http://omia.angis.org.au/OMIA001451/9913/","Congenital muscular dystonia 2"]
["Q0P5J6",92,"N","K","K1C27_BOVIN","KRT27","c.276C>G","http://omia.angis.org.au/OMIA000246/9913/","Curly hair, karakul-type"]
["A4IF69",311,"V","A","NHLC2_BOVIN","NHLRC2","na","http://omia.angis.org.au/OMIA002103/9913/","Developmental duplications"]
["Q6TGR1",210,"R","I","Q6TGR1_BOVIN","MITF","c.629G>T","http://omia.angis.org.au/OMIA001680/9913/","Dominant white with bilateral deafness"]
["P01246",200,"T","M","SOMA_BOVIN","GH1","C_to_T","http://omia.angis.org.au/OMIA001473/9913/","Dwarfism, growth-hormone deficiency"]
["Q5XQN5",478,"E","K","K2C5_BOVIN","KRT5","4051G>A","http://omia.angis.org.au/OMIA002081/9913/","Epidermolysis bullosa, simplex, KRT5-related"]
["B9X245",2153,"L","H","B9X245_BOVIN","F8","T>A","http://omia.angis.org.au/OMIA000437/9913/","Haemophilia A"]
["G5E556",1873,"H","R","G5E556_BOVIN","ABCA12","A5804G","http://omia.angis.org.au/OMIA000547/9913/","Ichthyosis congenita"]
["Q29451",321,"F","L","MA2B1_BOVIN","MAN2B1","T961>C","http://omia.angis.org.au/OMIA000625/9913/","Mannosidosis, alpha in Bos taurus"]
["Q29451",221,"R","H","MA2B1_BOVIN","MAN2B1","G662>A","http://omia.angis.org.au/OMIA000625/9913/","Mannosidosis, alpha in Bos taurus"]
["A6QM01",452,"E","K","A6QM01_BOVIN","NAGLU","c.1354G>A","http://omia.angis.org.au/OMIA001342/9913/","Mucopolysaccharidosis IIIB"]
["O18836",64,"L","P","GDF8_BOVIN","MSTN","c.191T>C","http://omia.angis.org.au/OMIA000683/9913/","Muscular hypertrophy (double muscling)"]
["Q4PKH3",750,"Y","Q","CLCN7_BOVIN","CLCN7","TAC>CAA","http://omia.angis.org.au/OMIA001887/9913/","Osteopetrosis with gingival hamartomas"]
["A7MBC5",79,"V","L","G3MWG4_BOVIN","IARS","c.235G>C","http://omia.angis.org.au/OMIA001817/9913/","Perinatal weak calf syndrome"]
["E1BE78",568,"S","N","E1BE78_BOVIN","PNPLA8","c.G1703A","http://omia.angis.org.au/OMIA000827/9913/","Progressive degenerative myeloencephalopathy (Weaver syndrome)"]
["Q0VCY0",211,"G","V","AT2A1_BOVIN","ATP2A1","c.632G>T","http://omia.angis.org.au/OMIA001464/9913/","Pseudomyotonia, congenital"]
["A2VDN5",560,"R","Q","SPAST_BOVIN","SPAST","na","http://omia.angis.org.au/OMIA001247/9913/","Spinal dysmyelination"]
["Q2KIJ5",175,"A","T","KDSR_BOVIN","KDSR","G-to-A","http://omia.angis.org.au/OMIA000939/9913/","Spinal muscular atrophy"]
["A6N9I4",234,"L","P","GRP2_BOVIN","RASGRP2","701T>C","http://omia.angis.org.au/OMIA001003/9913/","Thrombopathia"]
["F1MR49",66,"K","E","F1MR49_BOVIN","T","c.196A>G","omia.angis.org.au/OMIA001951/9913/","Vertebral and spinal dysplasia"]